I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT)— 510(k) K760263

Substantially Equivalent

Foregger

FDA 510(k) clearance K760263 for I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT), Substantially Equivalent on 1976-08-04. Applicant: Foregger. Device class: 2.

Clearance details

Applicant: Foregger
Product code: Code CBO
Device class: Class 2
Regulation: 21 CFR 868.5955
Advisory panel: Anesthesiology
Date received: 1976-07-21
Decision date: 1976-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CBO

K811991 — SIMVAC1981-08-12
K811908 — IMV MANIFOLDS1981-07-16
K791904 — IMV W/BAG & HOSES #M-5091979-10-09
K791905 — IMV W/BAG & TUBING #M-5081979-10-09
K791906 — IMV W/BAG #M-5071979-10-09

More clearances from Foregger

K771057 — ANESTHESIA MACHINE1977-07-05

Data sourced from openFDA. This site is unofficial and independent of the FDA.